Lead R&D Engineer

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Location:

​Libertyville​Department: ​Research & Development Summary The Lead R&D Engineer is a senior individual contributor within Research and Development who provides technical leadership in the identification, design, development, and commercialization of medical devices. The role applies strong engineering expertise to progress product concepts from early clinical need and technology exploration through prototype development, verification, validation, and support of commercialization. Operating with a high degree of autonomy, the Lead R&D Engineer collaborates extensively with cross‑functional partners across R&D, Quality, Regulatory, Manufacturing, and Marketing to deliver innovative, compliant, and customer‑focused solutions that support business growth.

Hollister Incorporated operates in a hybrid work environment. Associates are expected to come into the office in Libertyville, IL a minimum of 4 days per week. Responsibilities Represent Research and Development on cross‑functional product development and commercialization teams.

Translate basic clinical and customer needs into device concepts, designs, and prototypes while ensuring consideration of human factors, usability, and regulatory requirements.

Research, evaluate, and apply new materials, technologies, and processes to support development of new and existing product platforms.

Lead or support concept development, feasibility assessments, prototyping, and iterative design refinement.

Source, select, and evaluate materials, components, and supplier technologies for suitability and performance.

Develop product and component specifications to ensure consistent performance aligned to customer and business requirements.

Develop and execute test methods to characterize and measure product performance, stability, and functionality.

Plan, perform, and document design verification and design validation activities in compliance with design control requirements.

Provide technical R&D support to Global Marketing, Regulatory Affairs, Engineering, Manufacturing, and other functions as required.

Manage assigned project schedules, conduct technical and project risk analyses, and support timely completion of project deliverables.

Prepare and maintain technical documentation including reports, drawings, specifications, and analysis summaries.

Support intellectual property activities, including collaboration with patent counsel on patentability and infringement assessments.

Apply advanced engineering knowledge to solve complex and often ambiguous technical problems.

Lead or significantly contribute to technical execution of projects with minimal supervision.

Integrate regulatory, quality, and design control requirements into development activities.

Analyze experimental and performance data using appropriate analytical and statistical methods.

Communicate technical information clearly and effectively to cross‑functional stakeholders at multiple organizational levels.

Collaborate effectively within multidisciplinary teams and contribute to a culture of innovation, accountability, and continuous improvement.

Essential Functions of the Role Translating technical findings into business-relevant insights.
Drive continuous improvement initiatives.
Collaborate with cross-functional teams (Regulatory, Marketing, Market Access).
Ensuring adherence to regulatory standards (e.g., EU MDR, FDA).
Maintain quality systems and compliance with regulatory standards.
Education & Work Requirements Bachelor’s Degree with 8-12 years of related experience
Education & Work Preferences Honours Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Design Engineering, or a related engineering discipline required.

Typically requires…